3,4',5-Trihydroxy-3'-methoxystilbene

Details

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Internal ID a83c14ab-6039-4904-88d1-760b559740c8
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 5-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]benzene-1,3-diol
SMILES (Canonical) COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O
InChI InChI=1S/C15H14O4/c1-19-15-8-10(4-5-14(15)18)2-3-11-6-12(16)9-13(17)7-11/h2-9,16-18H,1H3
InChI Key ANNNBEZJTNCXHY-UHFFFAOYSA-N
Popularity 10 references in papers

Physical and Chemical Properties

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Molecular Formula C15H14O4
Molecular Weight 258.27 g/mol
Exact Mass 258.08920892 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 3.20
Atomic LogP (AlogP) 2.98
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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FT-0656349

2D Structure

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2D Structure of 3,4',5-Trihydroxy-3'-methoxystilbene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9682 96.82%
Caco-2 + 0.8305 83.05%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5713 57.13%
OATP2B1 inhibitior - 0.5741 57.41%
OATP1B1 inhibitior + 0.9607 96.07%
OATP1B3 inhibitior + 0.9785 97.85%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9338 93.38%
BSEP inhibitior - 0.4906 49.06%
P-glycoprotein inhibitior - 0.9170 91.70%
P-glycoprotein substrate - 0.9759 97.59%
CYP3A4 substrate - 0.6540 65.40%
CYP2C9 substrate - 0.5963 59.63%
CYP2D6 substrate - 0.6581 65.81%
CYP3A4 inhibition + 0.5185 51.85%
CYP2C9 inhibition + 0.8148 81.48%
CYP2C19 inhibition + 0.6868 68.68%
CYP2D6 inhibition - 0.8877 88.77%
CYP1A2 inhibition + 0.9192 91.92%
CYP2C8 inhibition + 0.6221 62.21%
CYP inhibitory promiscuity + 0.8813 88.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7994 79.94%
Carcinogenicity (trinary) Non-required 0.5977 59.77%
Eye corrosion - 0.9623 96.23%
Eye irritation + 0.9864 98.64%
Skin irritation - 0.5964 59.64%
Skin corrosion - 0.6008 60.08%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6025 60.25%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.6123 61.23%
skin sensitisation + 0.5135 51.35%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.7375 73.75%
Nephrotoxicity - 0.6034 60.34%
Acute Oral Toxicity (c) III 0.6130 61.30%
Estrogen receptor binding + 0.8601 86.01%
Androgen receptor binding + 0.6730 67.30%
Thyroid receptor binding + 0.6238 62.38%
Glucocorticoid receptor binding + 0.7670 76.70%
Aromatase binding + 0.8800 88.00%
PPAR gamma + 0.8264 82.64%
Honey bee toxicity - 0.9249 92.49%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9662 96.62%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.66% 91.11%
CHEMBL3194 P02766 Transthyretin 96.42% 90.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.95% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.72% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.98% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 89.58% 91.49%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.88% 89.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.51% 96.09%
CHEMBL4208 P20618 Proteasome component C5 83.68% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.29% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.29% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.80% 99.15%
CHEMBL2487 P05067 Beta amyloid A4 protein 81.48% 96.74%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.89% 90.24%
CHEMBL2535 P11166 Glucose transporter 80.22% 98.75%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Aiphanes horrida
Caragana tibetica
Gnetum hainanense
Gnetum klossii
Gnetum macrostachyum
Gnetum pendulum
Rheum rhabarbarum
Schizocarphus nervosus
Smilax corbularia

Cross-Links

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PubChem 53395093
NPASS NPC71715
LOTUS LTS0001470
wikiData Q104915303